Clinical Information Science Principal
AstraZeneca AB / Datajobb / Göteborg
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hela Sverige Clinical Information Science Principal, Respiratory / Inflammation Autoimmunity & Neuroscience
Location(s) - Gaithersburg (US); Gothenburg (SWE) - Permanent
Salary - Competitive salary and company benefits apply
At AstraZeneca every one of our employees makes a difference to patient lives every day. Each one of us believes that science has the ability to change lives and that to deliver this takes many people with many skill sets. When we deliver a life-changing medicine, that success comes from the combined efforts of all of our people.
Biometrics & Information Sciences (B&I) is the statistical and information experts home for late stage drug development driving use of internal and external information and knowledge in design and decision making driving late stage drug development (Phase 2 and beyond).
As a Clinical Information Science Principal (CISP) within Respiratory/Inflammation Autoimmunity & Neuroscience you will support clinical directors and clinical design teams in finding and structuring clinical information driving optimal designs for late stage drug development.
If you're inspired by the possibilities of science to make a difference and ready to discover what you can do - join us.
Main Duties and Responsibilities
As a key leader of Information Practice embedded within B&I you will blend your clinical drug development knowledge and computer tools knowledge to find key information. Embedded within fast moving drug project teams, you will efficiently scope and deliver the information clinical teams need to make decisions driving the drug development process. You will be embedded in drug project teams on projects transitioning into late phase development (Phase 2 and beyond), or into Established Brand teams.
You will access variety of internal and external information sources (ClinicalTrials.Gov, BioMed Tracker, internal clinical databases) identifying, extracting and sharing the information to inform key drug decisions necessary for clinical trials development.
You will also lead key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and stakeholders.
The significant areas for contribution are:
Clinical Design
* Support decision making in clinical design by identifying, extracting and presenting back relevant facts and data via internal and external information sources (ClinicalTrials.Gov, BioMed Tracker, internal clinical databases)
* Building a repository of key data capturing key historical decisions for wide team to use and refer to (build the memory of clinical trials ranging from Phase IIb thru registration and life cycle management)
* Lead the design team by liaising with project stakeholders to plan and schedule project timelines tracking project milestones
* Develop and control deadlines and prepare progress reports
Disseminate key clinical information
* Using techniques such as: text mining, data visualization, competitive intelligence, and benchmarking extract key relevant information proactively enabling clinical drug design decision makers to make timely and objective decisions
* Facilitate access to complex information for the drug project and ensure access to and (re)use of clinical information, documents and data
Essential Requirements
* Bachelors or advanced degree in a Life Science
* Knowledge of the pharmaceutical clinical drug development process (with a preference for late-stage drug development in Respiratory / Inflammation Autoimmunity & Neuroscience)
* Good understanding of project management techniques and methods
* Experience in clinical information or science information setting in the application of information and knowledge management (settings could include, but are not limited to clinical drug development, medical writing, medical affairs, clinical operations, competitive intelligence, regulatory intelligence)
* Good written and verbal communication skills
* Good organizational skills and the ability to multitask; can set priorities and follow a timeline
* Ideally a self-starter, who is capable of working independently
Next Steps - Apply today!
To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
Closing date for applications - 31 August 2018
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2018-07-13ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2018-07-30
Ange följande referens när du ansöker: R-032040
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
Caralina.Gille@astrazeneca.comFöretagAstraZeneca AB
AdressAstraZeneca AB
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 4251969
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